Mine Arslan‐Kirchner

5.0k total citations
39 papers, 891 citations indexed

About

Mine Arslan‐Kirchner is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Mine Arslan‐Kirchner has authored 39 papers receiving a total of 891 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 17 papers in Pulmonary and Respiratory Medicine and 11 papers in Molecular Biology. Recurrent topics in Mine Arslan‐Kirchner's work include Connective tissue disorders research (21 papers), Aortic Disease and Treatment Approaches (13 papers) and Cardiac Valve Diseases and Treatments (9 papers). Mine Arslan‐Kirchner is often cited by papers focused on Connective tissue disorders research (21 papers), Aortic Disease and Treatment Approaches (13 papers) and Cardiac Valve Diseases and Treatments (9 papers). Mine Arslan‐Kirchner collaborates with scholars based in Germany, Italy and United States. Mine Arslan‐Kirchner's co-authors include Jörg Schmidtke, Kathrin Rommel, Matthias Karck, Krishna K. Singh, Axel Haverich, Yskert Von Kodolitsch, Anjali Mishra, Meike Rybczynski, Sabrina Spengler and Gerhard Binder and has published in prestigious journals such as PEDIATRICS, Journal of Molecular and Cellular Cardiology and Genomics.

In The Last Decade

Mine Arslan‐Kirchner

39 papers receiving 861 citations

Peers

Countries citing papers authored by Mine Arslan‐Kirchner

Since Specialization

Citations

This map shows the geographic impact of Mine Arslan‐Kirchner's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mine Arslan‐Kirchner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mine Arslan‐Kirchner more than expected).

Fields of papers citing papers by Mine Arslan‐Kirchner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mine Arslan‐Kirchner. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mine Arslan‐Kirchner. The network helps show where Mine Arslan‐Kirchner may publish in the future.

Co-authorship network of co-authors of Mine Arslan‐Kirchner

This figure shows the co-authorship network connecting the top 25 collaborators of Mine Arslan‐Kirchner. A scholar is included among the top collaborators of Mine Arslan‐Kirchner based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mine Arslan‐Kirchner. Mine Arslan‐Kirchner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	NCAM2 deletion in a boy with macrocephaly and autism: Cause, association or predisposition? 2016 ·European Journal of Medical Genetics ·Caroline Scholz, Doris Steinemann, (unknown), Mandy Roy, Mine Arslan‐Kirchner, Thomas Illig, Jörg Schmidtke, Manfred Stuhrmann	13
2	Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches 2015 ·European Journal of Human Genetics ·Mine Arslan‐Kirchner, Eloisa Arbustini, Cathérine Boileau, Philippe Charron, Anne H. Child, Gwenaëlle Collod‐Béroud, Julie De Backer, Anne De Paepe, (unknown), Laurence Bonhomme‐Faivre, Sabine Hoffjan, Guillaume Jondeau, Britta Keyser, Bart Loeys, Karin Mayer, Peter N. Robinson, Jörg Schmidtke	17
3	Tetrasomie 18p und Innenohrschwerhörigkeit 2012 ·HNO ·C. Schwemmle, Mine Arslan‐Kirchner, Brigitte Pabst, M. Ptok	1
4	Analysis of phenotype and genotype information for the diagnosis of Marfan syndrome 2011 ·Clinical Genetics ·Sara Sheikhzadeh, (unknown), Britta Keyser, Manfred Stuhrmann, Mine Arslan‐Kirchner, Meike Rybczynski, (unknown), (unknown), Mathias Hillebrand, Thomas S. Mir, Peter N. Robinson, J. Berger, Christian Detter, Stefan Blankenberg, Jörg Schmidtke, Yskert Von Kodolitsch	38
5	Dural ectasia in individuals with Marfan-like features but exclusion of mutations in the genes FBN1, TGFBR1 and TGFBR2 2010 ·Clinical Genetics ·Sara Sheikhzadeh, Meike Rybczynski, (unknown), (unknown), Mine Arslan‐Kirchner, Britta Keyser, H. Kaemmerer, (unknown), A Staebler, (unknown), Peter N. Robinson, J. Berger, T. Meinertz, Yskert Von Kodolitsch	16
6	Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome 2010 ·European Journal of Medical Genetics ·(unknown), Bettina Bohnhorst, I. Luhmer, Susanne Morlot, Axel Bohring, Jon Jonasson, Jörg T. Epplen, Dorothea Gadzicki, Stefanie Glaser, Gudrun Göhring, (unknown), Anke Hein, Mine Arslan‐Kirchner, Manfred Stuhrmann, Jörg Schmidtke, Brigitte Pabst	14
7	Prognosis Factors in Probands With an FBN1 Mutation Diagnosed Before the Age of 1 Year 2010 ·Pediatric Research ·Chantal Stheneur, Laurence Faivre, Gwenaëlle Collod‐Béroud, Élodie Gautier, Christine Binquet, Claire Bonithon‐Kopp, Mireille Claustres, Anne H. Child, Eloisa Arbustini, Lesley C. Adès, Uta Francke, Karin Mayer, Mine Arslan‐Kirchner, Anne De Paepe, Bertrand Chevallier, Damien Bonnet, Guillaume Jondeau, Cathérine Boileau	55
8	Performance of a new quantitative method for assessing dural ectasia in patients with FBN1 mutations and clinical features of Marfan syndrome 2009 ·Neuroradiology ·(unknown), (unknown), Jana Prokein, H. Becker, Jörg Schmidtke, Mine Arslan‐Kirchner	8
9	The Importance of Genetic Testing in the Clinical Management of Patients With Marfan Syndrome and Related Disorders 2008 ·Deutsches Ärzteblatt international ·Mine Arslan‐Kirchner, Yskert Von Kodolitsch, Jörg Schmidtke	13
10	The spectrum of syndromes and manifestations in individuals screened for suspected Marfan syndrome 2008 ·American Journal of Medical Genetics Part A ·Meike Rybczynski, A. Bernhardt, U. Rehder, Bettina Fuisting, L. Meiss, Ursula Voss, Christian R. Habermann, Christian Detter, Peter N. Robinson, Mine Arslan‐Kirchner, Jörg Schmidtke, Thomas S. Mir, Jürgen Berger, Thomas Meinertz, Yskert Von Kodolitsch	65
11	Marfan syndrome: clinical consequences resulting from a medicolegal autopsy of a case of sudden death due to aortic rupture 2008 ·International Journal of Legal Medicine ·Michael Klintschar, Udo Bilkenroth, Mine Arslan‐Kirchner, J. Schmidtke, D Stiller	22
12	Identification of 29 novel and nine recurrent fibrillin-1 (FBN1) mutations and genotype-phenotype correlations in 76 patients with Marfan syndrome 2005 ·Human Mutation ·Kathrin Rommel, Matthias Karck, Axel Haverich, Yskert Von Kodolitsch, Meike Rybczynski, Götz Müller, Krishna K. Singh, Jörg Schmidtke, Mine Arslan‐Kirchner	78
13	Agenesis of the Corpus Callosum, Abnormal Genitalia and Intractable Epilepsy due to a Novel Familial Mutation in the Aristaless-Related Homeobox Gene 2004 ·Neuropediatrics ·Hans Hartmann, G. Uyanık, (unknown), Ute Hehr, Thomas Lücke, Mine Arslan‐Kirchner, (unknown), Anibh M. Das, Jürgen Winkler	23
14	The application of region-specific probes for the resolution of duplication 8p: a case report and a review of the literature 2003 ·Cytogenetic and Genome Research ·Brigitte Pabst, Mine Arslan‐Kirchner, Jörg Schmidtke, (unknown)	4
15	Search for deletion 22q11.2 in interphase nuclei of buccal mucosa of patients ascertained by isolated cleft palate: a new diagnostic approach 2003 ·International Journal of Oral and Maxillofacial Surgery ·(unknown), Brigitte Pabst, Mine Arslan‐Kirchner, A. Eckardt, R. Schönweiler, M. Ptok, Yasmin Mehraein, Jörg Schmidtke, (unknown)	8
16	Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin 2003 ·Human Genetics ·Konstantin Miller, Brigitte Pabst, (unknown), Peter Nürnberg, Reiner Siebert, Jörg Schmidtke, Mine Arslan‐Kirchner	12
17	Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria 2000 ·Pediatric Nephrology ·(unknown), (unknown), D. J. Byrd, Mine Arslan‐Kirchner, Udo Vester, Manfred Stuhrmann, Thilo Dörk, Kathrin Saar, André Reis, J. Schmidtke, J. Brodehl	9
18	A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patients 1999 ·European Journal of Pediatrics ·(unknown), I. Luhmer, Mine Arslan‐Kirchner, H. C. Kallfelz, Jörg Schmidtke	25
19	Recombinant Families Locate the Gene for Non-Type I Cystinuria between Markers C13 and D19S587 on Chromosome 19q13.1 1999 ·Genomics ·Lídia Feliubadaló, Luigi Bisceglia, Mariona Font, Luca Dello Strologo, Ercole Beccia, Mine Arslan‐Kirchner, Beat Steinmann, Leopoldo Zelante, Xavier Estivill, António Zorzano, Manuel Palacı́n, Paolo Gasparini, Virginia Nunes	10
20	Identification of 9 novel FBN1 mutations in German patients with Marfan syndrome 1999 ·Human Mutation ·Alice Abdel Aleem, Matthias Karck, Axel Haverich, Jörg Schmidtke, Mine Arslan‐Kirchner	14

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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